The "MCCC2 Gene 3-Methylcrotonyl-CoA Carboxylase 2 Deficiency Genetic Test" is a specialized diagnostic tool available at DNA Labs UAE, designed to identify mutations in the MCCC2 gene. These mutations can lead to 3-Methylcrotonyl-CoA Carboxylase 2 deficiency, a rare metabolic disorder that affects the body's ability to process certain proteins properly. This condition can lead to various health issues, including developmental delay, metabolic acidosis, and in some cases, life-threatening complications if not diagnosed and managed early.
The test involves collecting a DNA sample, usually through a blood draw or cheek swab, and analyzing it for specific genetic alterations associated with the disorder. The goal is to provide a definitive diagnosis, enabling targeted treatment and management plans to improve patient outcomes.
The cost of the MCCC2 Gene 3-Methylcrotonyl-CoA Carboxylase 2 Deficiency Genetic Test at DNA Labs UAE is set at 4400 AED. This investment covers the sophisticated genetic analysis required to detect the presence of mutations in the MCCC2 gene, offering peace of mind and critical health insights for affected individuals and their families.
The Chr. 15q11 Gene Prader-Willi Syndrome Genetic Test is a specialized diagnostic tool available at DNA Labs UAE, designed to detect abnormalities in the chromosome 15q11 region, which are associated with Prader-Willi Syndrome (PWS). PWS is a complex genetic condition that affects many parts of the body and is characterized by weak muscle tone (hypotonia), feeding difficulties in infancy, rapid weight gain and obesity beginning in childhood, intellectual disability, and often, behavioral problems.
This genetic test is crucial for early diagnosis and management of PWS, allowing for targeted interventions and support to improve the quality of life for individuals with the syndrome and their families. Conducted in the state-of-the-art facilities of DNA Labs UAE, the test involves analyzing the individual's DNA to look for specific genetic markers indicative of PWS, including deletions, uniparental disomy, or imprinting defects within the 15q11 region.
The cost of the Chr. 15q11 Gene Prader-Willi Syndrome Genetic Test is set at 4400 AED. This investment covers the comprehensive analysis necessary to accurately identify the genetic alterations associated with Prader-Willi Syndrome, providing families and healthcare providers with essential information for planning care and support.
The NDN Gene Prader-Willi Syndrome Genetic Test is a specialized diagnostic procedure aimed at detecting mutations in the NDN gene, which are associated with Prader-Willi Syndrome (PWS). This rare genetic disorder is characterized by a variety of symptoms, including reduced muscle tone, feeding difficulties in early infancy, rapid weight gain and obesity in early childhood, developmental delays, and sometimes, intellectual impairment. The test is crucial for early diagnosis and management of the condition, enabling healthcare providers to develop a comprehensive care plan tailored to the individual's needs.
Conducted at DNA Labs UAE, a leading facility in genetic testing, this test offers a reliable analysis for those suspected of having or carriers of the genetic markers for Prader-Willi Syndrome. With state-of-the-art technology and a team of expert geneticists, DNA Labs UAE ensures accurate and timely results. The cost of the NDN Gene Prader-Willi Syndrome Genetic Test is 4400 AED, reflecting the sophisticated nature of the genetic analysis and the invaluable insights it provides for affected individuals and their families. Early diagnosis through this test can significantly improve the quality of life for individuals with PWS by allowing for early intervention and support services.
The SNRPN gene plays a crucial role in the genetic testing for Prader-Willi Syndrome (PWS), a complex genetic disorder characterized by a variety of symptoms including developmental delays, poor muscle tone, feeding difficulties in infancy, and overeating in later childhood. This condition is caused by the loss of function of specific genes on chromosome 15, with the SNRPN gene being one of the key genes involved.
At DNA Labs UAE, individuals can undergo a genetic test specifically targeting the SNRPN gene to determine if they have Prader-Willi Syndrome. This test is particularly important for early diagnosis and intervention, which can significantly improve the quality of life for those affected by PWS. The process involves collecting a DNA sample, usually through a blood draw or a cheek swab, which is then analyzed in the laboratory for abnormalities associated with the SNRPN gene.
The cost of the SNRPN gene Prader-Willi Syndrome genetic test at DNA Labs UAE is 4400 AED. This price reflects the comprehensive nature of the test, including the sophisticated technology and expertise required to accurately identify mutations in the SNRPN gene. Early diagnosis through genetic testing can be a critical step in managing the symptoms of Prader-Willi Syndrome and providing the necessary support and treatments for those affected.
The TPM3 Gene Nemaline Myopathy Type 1 Genetic Test is a specialized diagnostic procedure offered by DNA Labs UAE, designed to identify mutations in the TPM3 gene, which are known to cause Nemaline Myopathy Type 1. This condition is a rare genetic disorder characterized by muscle weakness, hypotonia, and the presence of rod-like structures in muscle cells, which can affect individuals from infancy or childhood, leading to difficulties in walking, feeding, and breathing. The test involves analyzing the patient's DNA to detect any abnormalities in the TPM3 gene, providing crucial information for accurate diagnosis, management, and understanding of the disorder's progression. The cost of the test is set at 4400 AED, reflecting the intricate processes and advanced technology employed to ensure precise and reliable results. DNA Labs UAE, with its state-of-the-art facilities and expert team, ensures that patients receive comprehensive support throughout the testing process, from sample collection to result interpretation, aiding in the better management of Nemaline Myopathy Type 1.
The "IGBP1 Gene Corpus Callosum Agenesis with Mental Retardation, Ocular Coloboma, and Micrognathia Genetic Test" is a specialized diagnostic tool available at DNA Labs UAE. This test is designed to detect mutations in the IGBP1 gene, which have been associated with a rare congenital condition characterized by the absence or underdevelopment of the corpus callosum (the part of the brain that connects the two hemispheres), intellectual disabilities, ocular coloboma (a defect in the eye's iris or retina), and micrognathia (a condition where the jaw is significantly smaller than normal).
The test plays a crucial role in the early diagnosis and management of the condition, providing essential information for healthcare providers and families. By understanding the genetic underpinnings of these symptoms, medical professionals can offer more personalized care plans, anticipate potential complications, and provide genetic counseling to affected families.
The cost of the test is 4400 AED, reflecting the advanced technology and expertise required to accurately identify mutations in the IGBP1 gene. Conducted at DNA Labs UAE, a facility known for its state-of-the-art genetic testing services, patients and healthcare providers can expect reliable and comprehensive results that can significantly impact the management of this rare condition.
The Very Long Chain Fatty Acids (VLCFA) test is a specialized diagnostic examination aimed at measuring the levels of specific fatty acids in the body, which are crucial for various cellular functions, including energy production and the maintenance of cell membranes. This test is particularly significant in the detection and management of certain genetic metabolic disorders, such as X-linked adrenoleukodystrophy (X-ALD), which affects the nervous system and adrenal glands.
Performed at DNA Labs UAE, a leading facility renowned for its advanced diagnostic services, the VLCFA test is conducted through a blood sample. The process involves sophisticated laboratory techniques to accurately quantify the concentrations of very long chain fatty acids, providing essential insights into the metabolic functions of the patient.
The cost of the VLCFA test at DNA Labs UAE is set at 5100 AED. While the price might seem steep, the value of this test lies in its ability to offer critical data that can guide therapeutic strategies, potentially improving the quality of life for individuals with metabolic disorders. Patients considering this test are encouraged to consult with their healthcare provider to understand its relevance and implications fully.
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